Literature DB >> 10396197

Cone and rod dysfunction in the NARP syndrome.

I Chowers1, T Lerman-Sagie, O N Elpeleg, A Shaag, S Merin.   

Abstract

AIMS: Description of the ophthalmic manifestations of the NARP (neuropathy, ataxia, retinitis pigmentosa) syndrome that is associated with a point mutation in position 8993 of the mitochondrial DNA (mtDNA).
METHODS: A mother and her two children, all carrying the 8993 mtDNA mutation, were examined. Two had manifestations of the NARP syndrome. A complete ocular and systemic examination was performed on all three patients.
RESULTS: The clinical examination, electroretinogram, and visual fields revealed a typical cone-rod dystrophy in the son, and a typical cone dystrophy in the daughter. The mother had no ocular manifestations of the disease.
CONCLUSIONS: NARP is a recently described, maternally inherited mitochondrial syndrome in which a retinal dystrophy, among other abnormalities, is related to a mutation of the mtDNA at nucleotide 8993. This study demonstrates the great variability of the ocular manifestations in the NARP syndrome. It also indicates that the retinal dystrophy in at least some NARP patients affects primarily the cones.

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Year:  1999        PMID: 10396197      PMCID: PMC1722923          DOI: 10.1136/bjo.83.2.190

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  18 in total

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Authors:  T P KEARNS; G P SAYRE
Journal:  AMA Arch Ophthalmol       Date:  1958-08

2.  A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.

Authors:  I J Holt; A E Harding; R K Petty; J A Morgan-Hughes
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

3.  Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome.

Authors:  P Mäkelä-Bengs; A Suomalainen; A Majander; J Rapola; H Kalimo; A Nuutila; H Pihko
Journal:  Pediatr Res       Date:  1995-05       Impact factor: 3.756

4.  Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations.

Authors:  E K Nikoskelainen; K Huoponen; V Juvonen; T Lamminen; K Nummelin; M L Savontaus
Journal:  Ophthalmology       Date:  1996-03       Impact factor: 12.079

5.  Electrophysiologic tests in assessment of senile macular degeneration.

Authors:  M Marcus; S Merin; M Wolf; M Feinsod
Journal:  Ann Ophthalmol       Date:  1983-03

6.  Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.

Authors:  Y Tatuch; J Christodoulou; A Feigenbaum; J T Clarke; J Wherret; C Smith; N Rudd; R Petrova-Benedict; B H Robinson
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

7.  Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.

Authors:  C T Moraes; S DiMauro; M Zeviani; A Lombes; S Shanske; A F Miranda; H Nakase; E Bonilla; L C Werneck; S Servidei
Journal:  N Engl J Med       Date:  1989-05-18       Impact factor: 91.245

8.  The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three families.

Authors:  Y Tatuch; R A Pagon; B Vlcek; R Roberts; M Korson; B H Robinson
Journal:  Eur J Hum Genet       Date:  1994       Impact factor: 4.246

9.  Clinical subtypes of cone-rod dystrophy.

Authors:  J P Szlyk; G A Fishman; K R Alexander; N S Peachey; D J Derlacki
Journal:  Arch Ophthalmol       Date:  1993-06

10.  The retinal manifestations of mitochondrial myopathy. A study of 22 cases.

Authors:  M A Mullie; A E Harding; R K Petty; H Ikeda; J A Morgan-Hughes; M D Sanders
Journal:  Arch Ophthalmol       Date:  1985-12
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  3 in total

1.  Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.

Authors:  J E Sligh; S E Levy; K G Waymire; P Allard; D L Dillehay; S Nusinowitz; J R Heckenlively; G R MacGregor; D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-19       Impact factor: 11.205

2.  Adaptive optics scanning laser ophthalmoscopy images in a family with the mitochondrial DNA T8993C mutation.

Authors:  Michael K Yoon; Austin Roorda; Yuhua Zhang; Chiaki Nakanishi; Lee-Jun C Wong; Qing Zhang; Leslie Gillum; Ari Green; Jacque L Duncan
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-11-07       Impact factor: 4.799

Review 3.  Mitochondrial dysfunction in neurodegenerative diseases.

Authors:  Anthony H V Schapira
Journal:  Neurochem Res       Date:  2008-11-08       Impact factor: 3.996

  3 in total

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